Sodium Acetate Anhydrous Industrial White Crystalline Powder, 99% Purity for Material Evaluation
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ColorWhitePhysical formCrystalline , Powder
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CAS No.127-09-3Purity99%
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AppearanceWhite crystalApplicationWater Treatment, Food Additives, Textile Dyeing, P
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Intended useIndustrial UseEINECS No.204-823-8
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Molecular FormulaCH3COONaOther NamesAnhydrous Sodium Acetate
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TypeOtherProduct NameSodium Acetate Anhydrous
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Molecular Weight82.03Melting Point324°C
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Density1.53 g/cm³SolubilityEasily Soluble in Water
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MOQ1 MTPackaging25kg Bag, 500kg Bag, 1000kg Jumbo Bag
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Supply Ability3000 MT per MonthSampleAvailable
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CertificateCOA, MSDS, TDS, ISO
White crystalline material is the physical form to confirm when comparing this sodium acetate anhydrous offer. It identifies industrial use, 99% purity and CH3COONa formula, with TY-Sodium Acetate as the actual model designation.
Define the required crystalline powder characteristics
Ask for the physical measurements relevant to the project's material specification rather than relying on appearance alone. Pair those criteria with current assay, analytical method and impurity limits so the offered anhydrous acetate can be compared on a defined basis.
- Form check
- Confirm crystal or powder characteristics against the actual process requirements.
- Identity check
- Match the anhydrous designation, formula and chemical identifiers to current product records.
- Grade check
- Use actual analysis and agreed acceptance limits for the proposed material.
Relate the reported physical values to measurement methods
Density is stated as 1.53 g/cm3, with melting point reported at 324°C. Confirm the applicable methods and conditions; the qualitative easily-soluble-in-water description likewise needs relevant solution evidence when behaviour in a particular system matters.
Record acceptance for the intended industrial role
Water-treatment and textile-dyeing are identified directions, each requiring a proposed material function and representative process tests. Neither the chemical name nor the physical descriptors establish a universal process result or operating dose.
Current technical, analysis and safety documents should identify the actual offered crystals, and any ISO requirement needs its applicable certificate and scope. Keep this industrial enquiry within its confirmed grade evidence: purity or food-additives wording alone does not establish approval for food use.
